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2024
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Invention
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Combinatorial dna screening.
The present disclosure relates to a laboratory execution system tha... |
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Invention
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Systems and methods for automatically generating genetic risk assessments.
A computer-implemente... |
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Invention
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Laboratory execution and automation systems.
The present disclosure relates to a laboratory exec... |
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Invention
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Automated nucleic acid repeat count calling methods.
The present disclosure relates to processes... |
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Invention
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Systems and methods for inferring genetic ancestry from low-coverage genomic data.
A computer-im... |
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Invention
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Enrichment of circulating tumor dna.
The present disclosure relates to methods for detecting uni... |
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Invention
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Systems and methods for identifying and quantifying gene copy number variations.
A method of ide... |
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Invention
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Methods of preparing a dna fraction enriched with circulating tumor dna. The present disclosure r... |
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Invention
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Evaluation and improvement of genetic screening tests using receiver operating characteristic cur... |
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2023
|
Invention
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Noninvasive prenatal screening using dynamic iterative depth optimization.
Fetal maternal sample... |
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Invention
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Personalized methods for detecting circulating tumor dna. The present disclosure relates to a lab... |
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Invention
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Methods and compositions for preparing nucleic acid sequencing libraries.
Methods and compositio... |
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Invention
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Automated methods of detecting cell free dna. The present disclosure relates to a laboratory exec... |
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Invention
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Rna-facs for rare cell isolation and detection of genetic variants. The present disclosure provid... |
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Invention
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Nucleic acid sequencing adapters and uses thereof.
High-fidelity, high-throughput nucleic acid s... |
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Invention
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Non-invasive prenatal sample preparation and related methods and uses. The present disclosure rel... |
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Invention
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Non-invasive prenatal sample preparation and related methods and uses.
The present disclosure re... |
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2022
|
Invention
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Systems and methods for inferring genetic ancestry from low-coverage genomic data. A computer-imp... |
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Invention
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Methods and compositions for enrichment of target polynucleotides.
High-fidelity, high-throughpu... |
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Invention
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Enrichment of cell-free dna from a biological sample.
Provided are methods and compositions for ... |
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Invention
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Methods for identifying carrier status and assessing risk for spinal muscular atrophy.
Disclosed... |
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Invention
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Methods of detecting dna in a sample. The present disclosure relates to methods for detecting uni... |
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Invention
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System and methods for detecting genetic variation.
The invention provides methods, apparatuses,... |
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2021
|
Invention
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Copy number variant caller.
Direct targeted sequencing (DTS) methods and a hidden Markov model (... |
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Invention
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Bayesian sex caller.
A method and system for analyzing sex-chromosome aneuploidies of an individ... |
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Invention
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Bayesian sex caller. A method and system for analyzing sex-chromosome aneuploidies of an individu... |
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Invention
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Combinatorial dna screening. The present disclosure relates to methods for detecting unique genet... |
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Invention
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High-throughput sample processing systems and methods of use.
Disclosed herein are high-throughp... |
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Invention
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Nucleic acid sample enrichment and screening methods.
Described herein are methods for enriching... |
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Invention
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Nucleic acid sample enrichment and screening methods. Described herein are methods for enriching ... |
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Invention
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Reagent delivery and waste management system. Reagent delivery systems, which can include a reage... |
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2020
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Invention
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Copy number variant caller.
Described herein are methods of assessing a sample-specific performa... |
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Invention
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Deep learning based variant calling using machine learning.
A system and method for determining ... |
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Invention
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Variant calling using machine learning.
Methods for determining a respective carrier status of a... |
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Invention
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Method for determining genotypes in regions of high homology.
Described herein are methods direc... |
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Invention
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Methods and compositions for enrichment of target polynucleotides. High-fidelity, high-throughput... |
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Invention
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Methods and compositions for preparing nucleic acid sequencing libraries. Methods and composition... |
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Invention
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Method for detecting genetic variation in highly homologous sequences by independent alignment an... |
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2019
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Invention
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Automated nucleic acid repeat count calling methods. The present disclosure relates to processes ... |
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Invention
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Methods for optimizing direct targeted sequencing.
Described are methods for selecting an amount... |
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2018
|
Invention
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Noninvasive prenatal screening using dynamic iterative depth optimization with depth-scaled varia... |
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2017
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P/S
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Medical apparatus and instrument for diagnostic use, namely,
apparatus for medical diagnostic te... |
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P/S
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Medical diagnostic reagents and assays for testing of body fluids; medical diagnostic reagents, p... |
